Product code JAY— Anesthesiology
ADJUSTABLE TUBE TREE FOR ANESTH. HOSES
- Classification name
- Support, Breathing Tube
- Device class
- Class 1
- Regulation
- 21 CFR 868.5280
- Advisory panel
- Anesthesiology
- Total cleared
- 19
- First cleared
- Most recent
Market context for product code JAY
FDA has cleared devices under product code JAY between 1977 and 1995, filed by 14 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1995
- 1987
- 1986
- 1985
- 1984
- 1983
- 1980
- 1979
- 1978
- 1977
Top applicants under product code JAY
Recent clearances under product code JAY
- K944988 — CUSTOM MEDICAL SUSPENSION STRAP
- K873491 — BLOCK, BITE, INTUBATION
- K860583 — DALE HEAD BAND ANESTHESIA CIRCUIT TUBE HOLDER 1315
- K850924 — JEE FRAME (VENTILATOR CIRCUIT SUPPORT)
- K850309 — COMFIT PLUS ENDOTRACHEAL TUBE HOLDER & BITE BLOCK
- K840844 — ENDO-SECURE
- K834265 — TRACH MATE
- K834089 — COMFIT
- K833361 — TUBE-TITLE
- K833374 — BITE-BLOCK
- K833332 — SCHULTZ ENDHOLD
- K832946 — DALE ENDOTRACHEAL TUBE HOLDER
- K802675 — ENDOTRACHEAL TUBE HOLDER
- K792148 — ADJUSTABLE TUBE TREE FOR ANESTH. HOSES
- K791781 — TUBE-STRAP
- K790410 — ADULT ZEE-FRAME
- K781509 — ZEE-FRAME
- K770628 — CLAMP BE-152
- K770631 — FLEX ARM BE 122, CLAMP 122-27
Data sourced from openFDA. This site is unofficial and independent of the FDA.